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猪胸膜肺炎放线杆菌PCR检测方法的建立
引用本文:逯忠新,杨学山,赵卫平,赵萍,高鹏程,储岳峰.猪胸膜肺炎放线杆菌PCR检测方法的建立[J].中国兽医科学,2004,34(6):6-8.
作者姓名:逯忠新  杨学山  赵卫平  赵萍  高鹏程  储岳峰
作者单位:中国农业科学院,兰州兽医研究所,甘肃,兰州,730046
基金项目:国家“九五”重中之重攻关项目 (96 0 0 3 0 4 11 0 1)
摘    要:根据猪胸膜肺炎放线杆菌 (APP)外膜脂蛋白基因序列 ,设计合成了 1对特异性引物。经PCR扩增 ,APP 110标准血清型菌株均能扩增出大小为 980bp的DNA片段 ,而大肠埃希氏菌、猪多杀性巴氏杆菌、猪链球菌、猪肺炎霉形体和葡萄球菌等的扩增结果均为阴性。该方法检测APPDNA的敏感性可达 2pg。表明 ,此PCR方法特异性好 ,敏感性高 ,可用于猪传染性胸膜肺炎的快速诊断。

关 键 词:猪胸膜肺炎放线杆菌  PCR  外膜脂蛋白基因
文章编号:1000-6419(2004)06-0006-03
修稿时间:2004年2月25日

Establishment of PCR method for detection of Actinobacillus pleuropneumoniae
LU Zhong-xin,YANG Xue-shan,ZHAO Wei-ping,ZHAO Ping,GAO Peng-cheng,CHU Yue-feng.Establishment of PCR method for detection of Actinobacillus pleuropneumoniae[J].Veterinary Science in China,2004,34(6):6-8.
Authors:LU Zhong-xin  YANG Xue-shan  ZHAO Wei-ping  ZHAO Ping  GAO Peng-cheng  CHU Yue-feng
Abstract:According to nucleic acid sequence of outer membrane lipoprotein gene of Actinobacillus pleuropneumoniae (APP), a pair specific primers were designed. With the primers, DNA fragments 980 bp in length were amplified from 10 serotypes of APP standard strains by PCR. The sensibility of the PCR method is 2 pg. It was concluded from the above-mentioned results that the established PCR method can be used to diagnose quickly porcine infectious pleuropneumoniae.
Keywords:Actinobacillus pleuropneumoniae(APP)  PCR  outer membrane lipoprotein gene
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